Literature DB >> 23337217

A quantitative benefit-risk analysis of isoniazid for treatment of latent tuberculosis infection using incremental benefit framework.

Mohsen Sadatsafavi1, Carlo Marra, Fawziah Marra, Onofre Moran, J Mark FitzGerald, Larry Lynd.   

Abstract

BACKGROUND: We undertook a quantitative benefit-risk analysis of a targeted isoniazid (INH) therapy for latent tuberculosis (TB) infection for different groups of contacts of active TB cases.
METHODS: We developed a decision-analytic model to compare the treatment of latent TB infection in subgroups of contacts to no treatment over a 6-year time horizon in a Canadian setting. Contacts were stratified into 32 groups on the basis of five binary variables: type of contact (close or casual), tuberculin skin test (TST) results (positive or negative at 5 mm cutoff), Bacillus Calmette-Guérin vaccination status, place of birth (foreign- or Canadian-born), and age group (cutoff 35 years). Risk of TB reactivation was calculated for each subgroup from a longitudinal registry of contacts, adjusted for several potential confounders and comorbid conditions. We calculated the quality-adjusted life-years gained because of delayed or prevention of active TB via treatment of latent TB infection versus quality-adjusted life-years lost because of the adverse events to INH.
RESULTS: A targeted policy based on adopting INH therapy only in subgroups with positive expected incremental net health benefit resulted in a different treatment decision than the current guidelines in five subgroups comprising 3.9% of the contacts. Namely, the targeted policy comprised no INH therapy in casual contacts with a positive vaccination history even with a positive TST result and INH therapy in foreign-born close contacts younger than 35 years even with a negative TST result.
CONCLUSIONS: From a benefit-risk viewpoint, INH treatment of contacts should be tailored on the basis of risk assessment algorithms that consider a range of factors at the time of screening.
Copyright © 2013 International Society for Pharmacoeconomics and Outcomes Research (ISPOR). Published by Elsevier Inc. All rights reserved.

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Year:  2013        PMID: 23337217     DOI: 10.1016/j.jval.2012.09.006

Source DB:  PubMed          Journal:  Value Health        ISSN: 1098-3015            Impact factor:   5.725


  4 in total

Review 1.  Integration of PKPD relationships into benefit-risk analysis.

Authors:  Francesco Bellanti; Rob C van Wijk; Meindert Danhof; Oscar Della Pasqua
Journal:  Br J Clin Pharmacol       Date:  2015-07-29       Impact factor: 4.335

2.  Economic Evaluation of Multiple-Pharmacogenes Testing for the Prevention of Adverse Drug Reactions in People Living with HIV.

Authors:  Saowalak Turongkaravee; Naiyana Praditsitthikorn; Thundon Ngamprasertchai; Jiraphun Jittikoon; Surakameth Mahasirimongkol; Chonlaphat Sukasem; Wanvisa Udomsinprasert; Olivia Wu; Usa Chaikledkaew
Journal:  Clinicoecon Outcomes Res       Date:  2022-07-07

3.  Mathematical modelling of the impact of treating latent tuberculosis infection in the elderly in a city with intermediate tuberculosis burden.

Authors:  Ka Chun Chong; Chi Chiu Leung; Wing Wai Yew; Benny Chung Ying Zee; Greta Chun Huen Tam; Maggie Haitian Wang; Katherine Min Jia; Pui Hong Chung; Steven Yuk Fai Lau; Xiaoran Han; Eng Kiong Yeoh
Journal:  Sci Rep       Date:  2019-03-19       Impact factor: 4.379

4.  Cost-effectiveness of a Pharmacogenomic Test for Stratified Isoniazid Dosing in Treatment of Active Tuberculosis.

Authors:  Neil E Rens; Carin A Uyl-de Groot; Jeremy D Goldhaber-Fiebert; Julio Croda; Jason R Andrews
Journal:  Clin Infect Dis       Date:  2020-12-15       Impact factor: 9.079

  4 in total

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